Beschreibung
Start: asapDauer: 9 Monate
Beschreibung:
- Ensuring the data quality for regulatory submission
- Review of clinical study data, medical monitoring, and update of regulatory documents
- Advice on clinical development programs within clinical oncology
- Review of patient-level clinical study data provided in electronic format, medical monitoring according to processes provided in electronic format, update of regulatory documents provided in electronic format
Skills:
- Human physicians with a focus on oncology
- Relevant experience in the field of early clinical development in Oncology
- Advanced experience in reviewing clinical study data, medical monitoring, regulatory documents, regulatory submissions
- Fluent in English, German is an advantage
- Weekly capacity requested 50 %
- 50 % Onsite / 50 % Remote
- Duration of the project 6 to 9 months (Prolongation optional)